Canonical Allele Identifier: CA433593448
Gene: CCR5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.46414861T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.46373370T>A , CM000665.2:g.46373370T>A GRCh38
NC_000003.11:g.46414861T>A , CM000665.1:g.46414861T>A GRCh37
NC_000003.10:g.46389865T>A NCBI36
NG_012637.1:g.8229T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000292303.4:c.468T>A ENSP00000292303.4:p.Ala156=
ENST00000445772.1:c.468T>A ENSP00000404881.1:p.Ala156=
NM_000579.3:c.468T>A NP_000570.1:p.Ala156=
NM_001100168.1:c.468T>A NP_001093638.1:p.Ala156=
NR_125406.1:n.392-1953A>T
NM_000579.4:c.468T>A NP_000570.1:p.Ala156=
NM_001100168.2:c.468T>A NP_001093638.1:p.Ala156=